Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
  • C08L79/02—Polyamines
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
  • B32B27/283—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polysiloxanes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/04—Coating
  • C08J7/0427—Coating with only one layer of a composition containing a polymer binder
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/04—Coating
  • C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/04—Coating
  • C08J7/044—Forming conductive coatings; Forming coatings having anti-static properties
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/04—Coating
  • C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
  • C08J2367/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
  • C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds

Definitions

• the present invention relates to a laminated polyester film comprising an antistatic layer and a silicone resin layer.
• Laminates of a polyester film and a silicone resin layer are widely used as surface-hardening films, release films, slippery films, etc. in accordance with the property of the silicone resin, and an antistatic property is important in laminates as in general plastic films.
• a method of mixing a compound having an antistatic property with a silicone resin has already been proposed.
• the method of mixing a compound having an antistatic property involves problems that the crosslinking reactivity for forming a silicone resin layer is lowered, that the properties of the silicone resin layer such as transparency, surface hardness, releasability and slipperiness are deteriorated, and that the antistatic compound transfers to another base material with frequent use, thereby not only lowering the antistatic effect on the silicone resin layer but also contaminating the base material.
• a laminated polyester film which comprises (1) a film comprising a base polyester film and at least one polymer layer (A) comprising (a) a polymer having cationic nitrogens in the main chain thereof and (b) a binder polymer on one or both surfaces of the base polyester film, and (2) at least one polymer layer (B) comprising a silicone compound on one or both surfaces of the film comprising the base polyester film and at least one polymer layer (A).
• polyethylene terephthalate comprising 80 mol% or more of ethylene terephthalate unit and 20 mol% or less of the other copolymerized unit
• polyethylene naphthalate comprising 80 mol% or more of polyethylene naphthalate unit and 20 mol% or less of the other copolymerized unit
• poly-1,4-cyclohexanedimethylene terephthalate comprising 80 mol% of more of 1,4-cyclohexanedimethylene terephthalate unit and 20 mol% or less of the other copolymerized unit may be used.
• the base polyester film may contain inorganic particles, organic particles, an organic lubricant, an antisatic agent, a stabilizer, a dye, pigments, and an organic polymer, as occasion demands.
• fine particles are contained in base polyester films in order to impart slipping properties to the base polyester films, the type, size, and amount of the projection forming agent (fine particles) are appropriately selected in accordance with such properties and transparency demande for the product used.
• an ionene polymer may be mentioned.
• the ionene polymer is described in detail in Chapter 4 "IONENE POLYMERS: PREPARATION, PROPERTIES AND APPLICATIONS", ALAN D. WILSON AND HAVERD J. PROSSER (Ed.) "DEVELOPMENTS IN IONIC POLYMERS-2" ELSEVIER APPLEID SCIENCE PUBLISHERS, pp. 163-189, issued in 1986.
• an ionene polymer having a constitutional unit represented by the following formula (I) or (II) is preferably used: wherein X is bromine or chlorine; R1 and R2 independently represent alkylene groups, arylene groups, xylylene groups, divalent groups (A) derived from compounds selected from the group consisting of ethers, urea and derivatives thereof, piperadine and derivatives thereof, diacetoxypropane and derivatives thereof, and diethylbenzene, or diva lent groups (B) derived from compounds selected from the group consisting of polyacrylates, polyesters, polyurethanes, polyolefins, halogenated polyolefins and polyethylene glycol; said alkylene groups, said arylene groups, said xylylene groups and said divalent groups (A) may be substituted by a hydroxy group or a monovalent group derived from a compound selected from the group consisting of esters, ethers, alcohols, amides, urethane
• an ionene polymer having a constitutional unit represented by the following formula (III) is used: wherein X is bromine or chlorine; R1 and R2 independently represent C1-C4 alkylene groups, phenylene groups, xylylene groups, divalent groups derived from compounds selected from the group consisting of diethylethers and dipropylurea, and propylene groups substituted by a hydroxy group and n is an integer.
• X is a halogen element such as Br or Cl
• x and y are respectively any desired integer of 1 or more and may be either the same of different.
• X is a halogen element such as Br or Cl and n is any desired integer of 1 or more.
• R is the same divalent group as defined for R1 and R2 in formula (I).
• X is a halogen element such as Br or Cl and R is the same divalent group as defined for R1 and R2 in formula (I).
• x and y are respectively integers of 1 to 4.
• R4 is a monovalent group derived from any desired organic compound which may contain various functional groups and R5 is a divalent group derived from any desired organic compound.
• X is a halogen element such as Br or Cl, is a divalent group derived from various polymers and oligomers or the same divalent group as defined for R1 and R2 in formula (I).
• ionene polymers and derivatives thereof include the compounds disclosed in Japanese Patent Pubilication Nos. 53-23377 and 54-10039 and Japanese Patent Application Laid-Open (KOKAI) Nos. 47-34581, 56-76451, 58-93710, 61-18750 and 63-68687 and so on.
• the ionene polymers used in the present invention are not limited to these compounds.
• Examples of commercially available ionene products include the polymers having the structures given in Table 1 described below which are produced by Nihon Kasei Co. Ltd., but the ionene polymer products used in the present invention are not limited to these products.
• the polymer having cationic nitrogens in the main chain thereof used in the present invention has preferably a molecular weight of 1,000 to 100,000, more preferably 2,500 to 60,000.
• the polymer layer (A) contains an antistatically effective amount of the polymer having cationic nitrogens in the main chain thereof.
• the content of the polymer having cationic nitrogens in the main chain thereof in the polymer layer (A) is 5 to 95 wt%, preferably 10 to 50 wt%.
• the binder polymer (b) is a nonionic, cationic or ampho-ionic water-soluble organic polymer or a water-dispersible organic polymer which is used in the form of a cationic, nonionic or ampho-ionic water dispersion (hydrosol).
• binder polymer examples include water-soluble synthetic polymers such as polyvinyl alcohol, polyacrylamide, polyalkylene glycol, polyalkylene imine, polyallylamine, polyvinylpyrrolidones and the like; water-soluble semi-synthetic polymers such as methyl cellulose, hydroxyethyl cellulose and the like; and water-soluble natural polymers such as starch, saccharides (e.g., gum arabic, dextran, pullulan), proteins (e.g., glue, gelatin, casein) and the like.
• water-soluble synthetic polymers such as polyvinyl alcohol, polyacrylamide, polyalkylene glycol, polyalkylene imine, polyallylamine, polyvinylpyrrolidones and the like
• water-soluble semi-synthetic polymers such as methyl cellulose, hydroxyethyl cellulose and the like
• water-soluble natural polymers such as starch, saccharides (e.g., gum arabic, dextran, pullul
• binder polymer examples include water-dispersible organic polymers such as polyacrylate, polyurethane, polyester, chlorine-containing polymers (polyvinylidene chloride, polyvinyl chloride, chlorinated polyolefin, vinyl chloride-vinyl acetate copolymer, chloroprene, etc.), polyamide, styrene-butadiene rubber, polyolefine and modified polymers thereof.
• water-dispersible organic polymers such as polyacrylate, polyurethane, polyester, chlorine-containing polymers (polyvinylidene chloride, polyvinyl chloride, chlorinated polyolefin, vinyl chloride-vinyl acetate copolymer, chloroprene, etc.), polyamide, styrene-butadiene rubber, polyolefine and modified polymers thereof.
• the adhesion between the layer containing the binder polymer (the polymer layer (A)) and the layer containing a silicone compound (the polymer layer (B) such as a UV curable coating containing a silicone becomes more excellent.
• the water dispersion of the organic polymer may be obtained by dispersing the polymer which is modified to be hydrophilic by copolymerization with using a nonionic, cationic or ampho-ionic component as one of the comonomers. Also, the water dispersion may be obtained by forced emulsification of the polymer in the presence of a nonionic, cationic or ampho-ionic surfactant or by emulsion polymerization in the presence of a nonionic, cationic or ampho-ionic surfactant.
• a copolymer such as a random copolymer, a block copolymer and a graft copolymer or an aggregate of different polymers may be used.
• the copolymer include polyurethene-graft-polyacrylate and polyester-graft-polyacrylate which can be obtained by emulsion polymerization of acryl monomers in the presence of an aqueous solution or water dispersion of polyurethane or polyester.
• the content of the binder polymer in the polymer layer (A) is 5 to 95 wt%, preferably 60 to 80 wt%.
• the amount of the binder polymer in the polymer layer (A) is preferably 50 to 2,000 parts by weight, based on 100 parts by weight of the polymer having cationic nitrogens in the main chain thereof.
• the polymer layer (A) is formed by dissolving or dispersing the polymer having cationic nitrogens in the main chain thereof (a) and a binder polymer (b) in a medium to obtain a coating solution, coating a film with the coating solution and drying the coated film.
• the medium for the coating solution is preferably water, and an organic solvent such as an alcohol, Cellosolve, N-methylpyrrolidone may be mixed with the coating solution in order to improve the cohesion stability of the coating, the application property of the coating to the polyester film, the film-forming property of the coating and the like. Water is preferable as the means for the coating solution from the point of view of the operation safety on the coating applicator is maintained, an organic solvent may be used singly.
• the concentration of the polymers in the medium may be adjusted so that the coating solution can be easily coated on a polyester film without any particular limit.
• the applicator of the above-described coating solution is exemplified by a reverse-roll coater, a gravure coater, a rod coater and an air doctor coater which are described in "Coating Method” by Yuji Harasaki, published by Maki Shoten in 1979, but it is not restricted thereto.
• a method of coating the coating solution is not specified, but a "in-line coating method" in which the coating solution is coated during the production of a polyester film is known as a method of forming a high-quality coating layer at a low cost.
• the in-line coating method include a method in which a coating solution is coated on a non-stretched polyester film and the polyester film is then biaxially stretched successively or simultaneously; a method in which a coatng solution is coated on a monoaxially stretched polyester film and then stretched in the direction perpendicular to the direction of the previous monoaxial stretching; a method in which a coating solution is coated on a biaxially stretched polyester film and then further stretched in the transverse and/or machine direction.
• the above-described stretching process is preferably carried out at 60 to 130°C, and the stretch ratio is at least 4 times, preferably 6 to 20 times, in terms of ratio by area.
• the stretched film is subjected to heat treatment at 150 to 250°C.
• the stretched film is then 0.2 to 20% relaxed in the machine and transverse directions in the zone at the highest temperature of the heat treatment and/or a cooling zone at the outlet of the heat treatment.
• a preferable method is a method in which a coating solution is coated on a monoaxially stretched polyester film which is 2 to 6 times stretched by a roll stretching method at 60 to 130°C, and the monoaxially stretched polyester film is then 2 to 6 times stretched at 80 to 130°C in the direction perpendicular to the direction of the previous stretching after it has been appropriately dried or immediately after the coating without drying, and is subjected to heat treatment at 150 to 250°C for 1 to 600 seconds.
• the coating solution used in the present invention may be coated on either only one surface of the polyester film or both surfaces thereof.
• a coating layer is formed on the other surface by using a coating solution other than the coating solution used in the present invention, as occasion demands, so that other properties can be imparted to the polyester film of the present invention.
• the film may be subjected to chemical treatment or discharge before coating.
• the coating layer may be subjected to discharge treatment after it has been formed.
• the in-line coating method since the drying of the coating layer simultaneously with stretching is possible, it is very advantageous in comparison with a method of separately carrying out the biaxially stretching process and the coating (or coating and drying) process in that (i) it is unnecessary to provide a drying furnace exclusively for that purpose and (ii) since the number of times for rewinding and winding the film is reduced by one time the contamination of the film with dust is reduced.
• this method since it is possible to reduce the thickness of the coating layer in accordance with the stretching ratio, this method is excellent as a method of laminating a thin film on a base polyester film.
• the heat treatment is carried out in the mild conditions, for example, at a lower temperature, in a shorter treatment time, althogh the evaporation and the decomposition of the antistatic agent are suppressed and the antistatic effect is produced, the mechanical strength, dimension stability and the like of the film obtained are unsatisfactory in most cases.
• the polymer having cationic nitrogens in the main chain thereof in the present invention unexpectedly exhibit a stable antistaic effect, even after the film is satisfactorily subjected to the heat treatment.
• the thus-produced polyester film on which the polymer layer (A) is formed preferably has a thickness within the range of 3 to 500 ⁇ m, and the thickness of the polymer layer (A) is preferably 0.01 to 5 ⁇ m, more preferably 0.02 to 1 ⁇ m. If the thickness of the polymer layer (A) is less than 0.01 ⁇ m, unevenness occurs in the polymer layer (A) of products because uniform coating layers cannot be easily obtained, while if the thickness is over 5 ⁇ m, the handling of the films produced become difficult owing to the deterioration in the slipping properties.
• the coating solution for forming the polymer layer (A) preferably contains a crosslinking agent.
• the crosslinking agent include a alkylolated urea compound such as a methylolated urea compound, melamine compound, guanamine compound, acrylamide compound, polyamide compound, an epoxy compound, an aziridine compound, a block polyisocyanate, a silane coupling agent, a titanium coupling agent, a zirco-aluminate coupling agent, a heat-, peroxide- and light-reactive vinyl compound, photosensitive resin or the like.
• a crosslinking agent include a alkylolated urea compound such as a methylolated urea compound, melamine compound, guanamine compound, acrylamide compound, polyamide compound, an epoxy compound, an aziridine compound, a block polyisocyanate, a silane coupling agent, a titanium coupling agent, a zirco-aluminate coupling agent, a
• the crosslinking agent may be combined with the binder polymer in advance, for example, in the case that at least one of monomers of the binder polymer is a crosslinking agent or that a functional group in the binder polymer is reacted with the crosslinking agent.
• the crosslinking agent anti-blocking property, water resistance, solvent resistance, adhesion between the binder polymer layer and an upper coating layer, and mechanical strength of the coating layer are improved. Consequently, when an upper coating layer is coated on the coating layer, antistatic property is also exhibited on the upper coating layer. In addition, the antistatic property is improved as well as the adhesion with the upper coating layer.
• the content of the crosslinking agent is 0 to 10,000 parts by weight, preferably 5 to 200 parts by weight, based on 100 parts by weight of the polymer having cationic nitrogens in the main chain thereof.
• the coating solution may contain particles of an inorganic compound such as silica, silica sol, alumina, alumina sol, zirconium sol, kaolin, talc, calcium carbonate, titanium oxide, a barium salt, carbon black, molybdenum sulfide, antimony oxide sol or the like for the purpose of improving the anti-blocking properties and slipping properties.
• an inorganic compound such as silica, silica sol, alumina, alumina sol, zirconium sol, kaolin, talc, calcium carbonate, titanium oxide, a barium salt, carbon black, molybdenum sulfide, antimony oxide sol or the like for the purpose of improving the anti-blocking properties and slipping properties.
• the content of the inorganic particles is 0 to 1,000 parts by weight, preferably 0.01 to 500 parts by weight, based on 100 parts by weight of the polymer having cationic nitrogens in the main chain thereof.
• the coating solution may contain an antifoaming agent, a coating properties modifier, a thickening agent, an organic lubricant, organic polymer particles, an antioxidant, an ultraviolet absorber, a foaming agent, a dye and so on, as occasion demands.
• the coating solution may also contain a polymer other than the polymers in the present invention in order to improve the properties of the coating solution or the coating layer.
• the silicone compound which is contained in the polymer layer (B) is a compound which is mainly composed of organopolysiloxane, such as silicone oil, silicone rubber and silicone resin.
• the organopolysiloxane may be straight-chain or crosslinked.
• the structure and degree of the crosslinking are appropriately selected depending upon the purpose of use. For example, a high degree of crosslinking is not always necessary for the purpose of obtaining the slipperiness or the releasability, and it is necessary to enhance the degree of crosslinking in the case that it is used for surface hardening in which the scuff resistance is required.
• silicone compound examples include condensates of organoalkoxysilane, such as polydimethylsiloxane and an organopolysiloxane represented by the following formula:
• organopolysiloxane having a three-dimensional crosslinked structure which is produced by the self condensation of silanol obtained by the hydrolysis of organoalkoxysilane is preferable.
• organopolysiloxane are represent by the following four types of structural units:
• Organopolysiloxanes have various structures which are represented by combination of these structural units. Especially, when organopolysiloxane is used for the purpose of improving the surface hardness, a three-dimensional reticulate polysiloxane having a structure represented by the combination of trifunctional structural units and tetrafunctional unit such as shown below is preferable:
• organopolysiloxane There are three types of organopolysiloxane:
• a carbon functional silane has a specific nature due to possession of both organic combination and inorganic combination. Since a silicon functional silane has few organic combinations, it has poor adhesion with a plastic base and it is brittle in spite of the high surface hardness. In contrast, a carbon functional silane is excellent in the adhesion with a plastic base as is obvious from examples in which it is used itself as a primer for improving the adhesion, and the surface hardness thereof is also excellent equally in various evaluations. On the other hand, a carbon functional silane is defective in that it is influenced by light, water, heat or the like in some organic combinations and has problems in the durability of the coating film and in that curing reaction requires a higher temperature and a longer time than the curing reaction of a silicon functional silane.
• a suitable silicone compound is selected in accordance with the purpose of the use.
• a silicone compound can be used as a releasing agent with reference to, for example, "Adhesion” vol. 28, No. 11, pp. 484-489 (1984).
• Silicone compounds are commercially available as the products of Dow Chemical, Shin-etsu Chemical Industry Co., Ltd., Toshiba Silicone Co., Ltd., Toray Silicone Co., Ltd., Sumitomo Chemical Co., Ltd., Daicel Ltd., Nihon Seika, Daihachi Chemical Ind. Corp., etc. These products are usable for the polymer layer (B) in the present invention but the polymer layer (B) is not restricted thereto.
• the polymer layer (B) contains an effective amount of the silicone compound for exhibiting slipperiness, releasability, heat resistance, etc. Ordinarily, the content of the silicone compound in the polymer layer (B) is 1 to 100 wt%.
• the polymer layer (B) may contain an organic polymer. Especially, when a low-molecular weight silicone compound such as silicone oil is used, the use of the organic polymer is preferable.
• organic polymer examples include polyester, polyacrylate, polyurethane, polyamide, polyimide, styrene-butadiene rubber (SBR), acrylonitrile-butadiene rubber (NBR), polyvinyl acetate, a chlorine-containing polymer (e.g., polyvinylidene chloride, polyvinyl chloride, vinyl chloride-vinyl acetate copolymer, chlorinated polyethylene).
• SBR styrene-butadiene rubber
• NBR acrylonitrile-butadiene rubber
• polyvinyl acetate examples include polyester, polyacrylate, polyurethane, polyamide, polyimide, styrene-butadiene rubber (SBR), acrylonitrile-butadiene rubber (NBR), polyvinyl acetate, a chlorine-containing polymer (e.g., polyvinylidene chloride, polyvinyl chloride, vinyl chloride-vinyl acetate copolymer
• the content of the organic polymer in the polymer layer (B) is preferably 0 to 99 wt%. Especially, when the organic polymer is used with a low-molecular weight silicone compound (having a molecular weight of not more than about 1,000), the content of the organic polymer in the polymer layer (B) is preferable 70 to 99 wt%.
• the amount of the organic polymer in the polymer layer (B) is preferably 0 to 10,000 parts by weight, based on 100 parts by weight of the silicone compound.
• the polymer layer (B) may contain a catalyst, a crosslinking agent, organic or inorganic fine particles, an application property modifier, a coloring agent, a stabilizer, a lubricant, etc., if necessary.
• the polymer layer (B) may be formed by coating a coating solution containing the above-described silicone compound by a conventional method. For example, methods which are described in "The Coating Process" by Yuji Harasaki are mentioned. Also, the polymer layer (B) may be laminated by an in-line coating method in the same way as in the polymer layer (A).
• the coating layer may be subjected to heat treatment (heat curing) so as to enhance the degree of crosslinking of the silicone compound(s).
• heat treatment heat curing
• the heat treatment is ordinarily carried out at 80 to 170°C and for 1 to 120 seconds.
• the polymer layer (B) may be formed by coating a coating solution containing organosilicon compounds and crosslinking the organosilicon compounds.
• a silicone coating which is mainly composed of a trifunctional component such as methyltrimethoxysilane is mentioned.
• the silicone coating which is mainly composed of the trifunctional component it can be modified to impart flexibility to the coating layer by an addition of a bifunctional compound such as dimethyldimethoxysilane to enhance the hardness of the coating layer by an addition of a tetramethoxysilane.
• a method of enhancing the hardness by adding colloidal silica to methyltrimethoxysilane has recently been proposed.
• the thickness of the polymer layer (B) is preferably in the range of 0.03 to 5 ⁇ m, more preferably in the range of 0.05 to 1 ⁇ m. A thickness of less than 0.03 ⁇ m tends to be too small to provide sufficient properties. A thickness of more than 5 ⁇ m tends to be unfavorable since the silicone compound tends to transfer due to insufficient curing.
• the composite film of the present invention have the following five types of layer structures: Polymer layer (B)/Polymer layer (A)/Base polyester film; Polymer layer (A)/Base polyester film/Polymer layer (B); Polymer layer (A)/Base polyester film/Polymer layer (A)/Polymer layer (B); Polymer layer (B)/Base polyester film/Polymer layer (A)/Polymer layer (B); and Polymer layer (B)/Polymer layer (A)/Base polyester film/Polymer layer (A) /Polymer layer (B).
• Each of the above-described layers may be laminated through an intermediate layer which imparts an adhesion or various other properties. It is possible to laminate a layer which imparts other function to the composite film. for example, an adhesion modifying layer obtained by applying a water dispersion of polyurethane containing an anionic group, which is described in Japanese Patent Application Laid-Open (KOKAI) No. 62-97890 (1987).
• the laminated polyester film of the present invention has excellent properties such as heat resistance, slipperiness, scuff resistance and releasability as well as antistatic property and can be used for various purposes, for example, as a thermal transfer film, a surface hardening or release film, a liner sheet for a tape cassette and a slip sheet.
• the turbidity of the film was measured by a separate type turbidimeter (NDH-20D (trade name); produced by Nihon Denshoku Kogyo) in accordance with JIS-K6714 and the transparency was evaluated by the measured turbidity.
• Two films each cut into a width of 15 mm and length of 150 mm were laminated on a flat glass plate.
• a rubber plate was placed on the upper film and a load was placed on the rubber plate.
• the two films were slipped on each other at a contact pressure of 2 g/cm2 and a speed of 20 mm/min to measure the frictional force.
• the friction coefficient immediately before slipping was regarded as a static friction coefficient ( ⁇ s) and the friction coefficient at the point which is 5 mm distant from the starting point was regarded as a dynamic frictional coefficient ( ⁇ d).
• the measuring atmosphere was 23°C and 50% RH.
• a concentric electrode 16008A (trade name); produced by Yokokawa Hewlett Packard) having an inner electrode of 50 mm in diameter and an outer electrode of 70 mm in diameter was placed on the sample in an atmosphere of 23°C and 50% RH.
• a voltage of 100 V was applied between the electrodes to measure the surface resistivity of the sample by a high-resistance meter (4329A (trade name); produced by Yokokawa Hewlett Packard).
• the film was electrified by rubbing a finger covered with gauze along the surface of the sample in ten reciprocations in an atmosphere of 23°C and 50% RH.
• the sample was brought close to fine silica particles Siloid 150 (trade name; produced by Fuji Davisson) and the distance at which the fine particles was adsorbed by the film was measured. Judgment was made on the basis of the following criteria:
• this test also serves as the evaluation of the strength of the coating film.
• Cellophane tape having a width of 18 mm produced by Nichiban Co., Ltd. was pasted in a length of 7 cm on the surface of the film in such a manner as not to produce any air bubble between the tape and the surface of the film.
• a constant load was applied to the cellophane tape by a manual loading roll of 3 kg. Thereafter, the cellophane tape was manually torn off from one end and the releasability was evaluated on the basis of the following criteria:
• Polyethylene terephthalate having an intrinsic viscosity of 0.65 was melt-extruded at a temperature of 280 to 300°C and cast on a cooling drum by an electrostatic contact method to obtain an amorphous film with a thickness of 415 ⁇ m
• the film was then stretched by 3.3 times in the machine direction at 95°C and each of the coating solutions having compositions shown in Table 2 was coated on a surface of the stretched film.
• the substances of the abrreviations in Table 2 are shown in Table 3.
• Each of the coated films was stretched by 3.3 times in the transverse direction at 110°C and was subjected to heat treatment at 210°C.
• Each of the obtained films comprises a base polyester film having a thickness of 38 ⁇ m and a coating layer (polymer layer (A)) having a thickness shown in Table 2.
• a coating layer (polymer layer (A)) having a thickness shown in Table 2.
• silicone resin coatings having compositions shown in Table 2 was then coated on the polymer layer (A) of the film.
• Each of the films was dried and subjected to heat treatment to obtain film comprising a silicone resin layer (polymer layer (B)) having a thickness of 0.06 ⁇ m.
• the properties of the films were evaluated and the results are shown in Table 4.
• the films obtained in Examples 1 to 4 were excellent in both antistatic property and releasability.
• the films had a haze of not more than 8% and no problem in practical use as to transparency. They were able to used without any problem as the release films which were unlikely to attract dust and the liner sheets for tape cassettes.
• the liner sheet of a commercially available tape cassette was removed and one of the films of Examples 1 to 4 which were processed in to liner sheets was incorporated into the tape cassette such that the surface of the polymer layer (B) was in contact with the section of the magnetic tape. Any of the liner sheets had a good slipperiness with the magnetic tape and exhibited a stable traveling property. Since the films were unlikely to attract dust, there was little contamination in the process for processing the films into the liner sheets, the films did not attract dust in the tape cassette and exhibited a stable traveling property over a long period.
• Polyethylene terephthalate having an intrinsic viscosity of 0.65 was melt extruded at a temperature of 280 to 300°C and cast on a cooling drum by an electrostatic contact method to obtain an amorphous film having a thickness of 415 ⁇ m.
• This films was stretched by 3.3 times in the machine direction at 95°C and further stretched by 3.3 times in the transverse direction at 110°C.
• the thus-stretched film was heat treated at 210°C to obtain a biaxially oriented polyester films having a thickness of 38 ⁇ m.
• the film obtained was transparent but there was no antistatic property or releasability, as shown in Table 3.
• a silicone resin coating (toluene/methylethyl ketone mixed solution) having a composition shown in Table 2 was coated to a surface of the film obtained in Comparative Example 1. After the film was dried, it was heat treated. Thus a polymer layer (B) having a thickness of 0.06 ⁇ m was laminated on the film.
• the substances of the abrreviations in Table 2 are shown in Table 3.
• the film obtained was excellent in releasability but poor in antistatic property, as shown in Table 4.
• a coating solution having the composition shown in Table 2 was coated on a surface of the polyester film after being stretched in stretched in the machine direction and before being stretched in the transverse direction in Comparative Example 1. Thereafter, in the same way as in Comparative Example 1, a film consisting of a base polyester film having a thickness of 38 ⁇ m and a coating layer having a thickness of 0.15 ⁇ m was obtained. The film obtained was excellent in antistatic property.
• a silicone resin coating having the composition shown in Table 2 was then coated on the coating layer of the film. After the film was dried, it was heat treated. Thus a polymer layer (B) having a thickness of 0.06 ⁇ m was laminated on the film. The film obtained was excellent in releasability but poor in the antistatic property, as shown in Table 4. This is assumed to be due to the poor solvent resistance of the antistatic agent and the dispersion in the polymer layer (B).
• the film was coated and stretched by using a coating solution having the composition shown in Table 2 in the same way as in Comparative Example 3. However, the film gave off a smell of amine while stretching the film in the transverse direct ion and heat setting it, and it was found that the nitrogen component in the antistatic agent was being decomposed and evaporated. The film obtained exhibited no antistatic property.
• a silicone resin coating having the composition shown in Table 2 was applied to the coating layer of the film and treated in the same way as in Comparative Example 3 to form the polymer layer (B) having a thickness of 0.06 ⁇ m. Only releasability was imparted to the film obtained, as shown in Table 4.
• Polyethylene terephthalate having an intrinsic viscosity of 0.65 was melt extruded at a temperature of 280 to 300°C and cast on a cooling drum by an electrostatic contact method to obtain an amorphous film having a thickness of 55 ⁇ m.
• This film was stretched by 3.3 times in the machine direction at 95°C and a coating solution having the same composition as Example 4 shown in Table 2 was coated on a surface of the stretched film.
• the coated film was further stretched by 4.0 times in the transverse direction at 110°C and heat treated at 210°C to obtain a film consisting of a base polyester film having a thickness of 5 ⁇ m and a coating layer (polymer layer (A)) having a thickness of 0.15 ⁇ m.
• a toluene/methylethyl ketone mixed solution of an acrylsilicone graft polymer ("Aron GS-30"; produced by Toa Gosei Chemical Industry Co., Ltd.), which was obtained by the graft polymerization of a methyl methacrylate resin as the main chain and polydimethylsiloxane in the ratio of about 10 : 1, was coated on the polymer layer (A) of the film, heated and dried to form a polymer layer (B) having a thickness of 0.2 ⁇ m.
• the film obtained exhibited a good antistatic property.
• the surface of the film on the opposite side of the coating layer was subjected to hot-melt coating with a hot-melt ink consisting of paraffin wax and carbon black, to obtain an ink layer having a thickness of 3 ⁇ m, thereby producing an ink donor film for thermal transfer.
• a hot-melt ink consisting of paraffin wax and carbon black
• the ink donor film obtained was free from the problems such as the adhesion of the films due to static electricity, discharge and nonuniformity in ink coating during the lamination of the polymer layer (B) and the hot-melt ink and during processing.
• the ink donor film also exhibited a good antistatic property in the form of a roll and a stable traveling property.
• the sticking property of the surface (the surface of the polymer layer (B)) of the film for thermal transfer which was in contact with the thermal head was evaluated by printing by a thermal printing apparatus produced by Matsushita Electronics Parts, Ltd. at a thermal head resistivity of 275 ⁇ , applied voltage of 13.7 V and a pulse width of 1.2 msec, no sticking phenomenon was observed.
• the sticking property was evaluated the same way by printing by a facsimile machine (Telecopia Model 245; produced by fuji Xerox Co., Ltd.), no sticking phenomenon was observed.
• the traveling property at this time had not problem in practical use.
• An ink donor film for thermal transfer was produced in the same way as in Example 5 except that no antistatic layer was laminated.
• the sticking preventive property as an ink donor film was almost the same as in Example 5, but the ink donor film was electrified so that the film easily stuck to the printed paper and the traveling property was slightly unstable.
• Adhesion of dust caused a printing miss.
• the ink donor film was unsuitable for practical use.
• Example 1 Laminated films were produced in the same way as in Example 1.
• the polymer layer (A) was formed by the in-line coating method, and the polymer layer (B) was then laminated thereon.
• Example 6 the polymer layer (A) was formed on a surface of the film and the polymer layer (B) was formed on the opposite side.
• Example 7 the polymer layer (A) was formed on both side of the film by a in-line coating method and the polymer layer (B) was laminated on the polymer layer on a single side of the film.
• the polymer layers (B) were laminated on the polymer layers (A) on both sides of the film.

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• 1990
  • 1990-03-07 JP JP2056213A patent/JPH03256741A/ja active Pending
• 1991
  • 1991-03-05 DE DE69119939T patent/DE69119939T2/de not_active Expired - Fee Related
  • 1991-03-05 EP EP91103338A patent/EP0445744B1/de not_active Expired - Lifetime
  • 1991-03-06 KR KR91003738A patent/KR960008296B1/ko not_active IP Right Cessation

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